Dubreuil J D, Fairbrother J M, Lallier R, Larivière S
Groupe de Recherche sur les Maladies Infectieuses du Porc (GREMIP), Faculté de Médecine Vétérinaire, Université de Montréal, St.-Hyacinthe, Québec, Canada.
Infect Immun. 1991 Jan;59(1):198-203. doi: 10.1128/iai.59.1.198-203.1991.
Production of heat-stable enterotoxin b (STb) by porcine Escherichia coli strains belonging to serogroup O115 was evaluated in ligated intestinal segments of adult rats. The conditions for optimal production and detection of STb were studied by using the STb-producing strain 4247. As STb production was similar in complex Trypticase soy broth and minimal Davis medium, the latter was used for the fermentation of strain 4247 and the production of STb in large quantities. STb was then purified to apparent homogeneity by sequential ultrafiltration, ultracentrifugation, and preparative gel electrophoresis. The enterotoxin was purified more than 500-fold and exhibited a molecular weight of approximately 5,000 as determined by urea-sodium dodecyl sulfate gel electrophoresis. Purified STb retained such chemical characteristics as resistance to heating (60 degrees C/30 min) and sensitivity to trypsin. A rabbit polyclonal antiserum was produced against the purified toxin. Numerous booster doses were required to obtain a significant enzyme-linked immunosorbent assay titer, suggesting that STb is a poor immunogen. Nevertheless, the antiserum was used successfully to discriminate between culture supernatants of STb-positive and STb-negative O115 E. coli strains, thus demonstrating the immunogenicity of purified STb.
对属于O115血清群的猪源大肠杆菌菌株产生热稳定肠毒素b(STb)的情况在成年大鼠的结扎肠段中进行了评估。使用产STb的菌株4247研究了STb最佳产生和检测的条件。由于在复杂的胰蛋白酶大豆肉汤和基本的戴维斯培养基中STb的产生情况相似,因此后者用于菌株4247的发酵和大量生产STb。然后通过连续超滤、超速离心和制备性凝胶电泳将STb纯化至表观均一。通过尿素 - 十二烷基硫酸钠凝胶电泳测定,该肠毒素纯化了500多倍,分子量约为5000。纯化的STb保留了对加热(60℃/30分钟)的抗性和对胰蛋白酶的敏感性等化学特性。制备了针对纯化毒素的兔多克隆抗血清。需要多次加强剂量才能获得显著的酶联免疫吸附测定效价,这表明STb是一种弱免疫原。然而,该抗血清成功用于区分STb阳性和STb阴性O115大肠杆菌菌株的培养上清液,从而证明了纯化STb的免疫原性。